DURALOC 1220-28-160Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295015215), received between Dec 1, 2017 and Mar 6, 2026 — classified as 7 injuries.

The most frequently reported specific device problem is “Naturally Worn” (4 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryMar 6, 2026Naturally Worn

  IT WAS REPORTED THE LEFT INLAY WAS WORN OUT.

  Patient problems: Insufficient Information

  MAUDE report 24532104 ↗
• InjuryJan 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO PAIN. DOI: UNKNOWN. DOR: (B)(6) 2024. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Pain

  MAUDE report 21069648 ↗
• InjuryFeb 2, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT WAS REVISED WITH RIGHT TOTAL HIP DUE TO PAIN RELATING TO FALLING. THE HEAD AND LINER WAS EXCHANGED. SURGICAL DELAY UNKNOWN. DOI: UNKNOWN ,DOR: ON (B)(6) 2024, AFFECTED SIDE: RIGHT HIP.

  Patient problems: Fall; Pain

  MAUDE report 18632130 ↗
• InjuryNov 20, 2023Device Dislodged or Dislocated; Naturally Worn; Device Dislodged or Dislocated; Naturally Worn

  IT WAS REPORTED THAT THE PATIENT'S HIP WAS ORIGINALLY DONE SEVERAL YEARS AGO. PATIENT BEING REVISED DUE TO HIP DISLOCATION. X-RAY SHOWS THE POLY WAS WORN SURGEON FELT PATIENT WOULD BENEFIT FROM A HEAD AND LINER EXCHANGE. A 60X28 10 DEGREE LINER WAS REMOVED, AND A 60X36 +4/10 DEGREE LINER WAS IMPLANTED. TRIAL REDUCTION PERFORMED WITH 36 +8.5 HEAD AND FOUND TO BE STABLE. DOI: UNKNOWN. DOR: (B)(6) 2023. AFFECTED SIDE : RIGHT HIP.

  Patient problems: Joint Dislocation

  MAUDE report 18174244 ↗
• InjuryJun 30, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS PAIN. ORIGINAL IMPLANT DATE UNKNOWN. DOI: UNKNOWN, DOR: (B)(6) 2020, LEFT SIDE.

  Patient problems: No Code Available; Pain

  MAUDE report 10210579 ↗
• InjuryNov 26, 2019Naturally Worn; Naturally Worn

  IT WAS REPORTED THAT THE DURALOC LINER SHOWED ECCENTRIC WEAR ON X-RAY. SURGEON REMOVED WORN DURALOC LINER AND REPLACED WITH A NEW LINER. THE HEAD WAS ALSO REPLACED. DOI: MORE THAN 20 YEARS; DOR: (B)(6) 2019; LEFT HIP.

  Patient problems: No Code Available

  MAUDE report 9376703 ↗
• InjuryDec 1, 2017Naturally Worn; Naturally Worn

  PATIENT WAS REVISED TO ADDRESS PAIN AND POLYWEAR.

  Patient problems: Pain

  MAUDE report 7074352 ↗